Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1992 Feb;447:191–213. doi: 10.1113/jphysiol.1992.sp018998

On the mechanism of action of picrotoxin on GABA receptor channels in dissociated sympathetic neurones of the rat.

C F Newland 1, S G Cull-Candy 1
PMCID: PMC1176032  PMID: 1317428

Abstract

1. The mechanism of action of picrotoxin on GABA receptor channels in rat sympathetic neurones has been investigated with whole-cell clamp. In addition, the action of picrotoxin on single GABA channels has been examined in outside-out membrane patches from these cells. 2. Picrotoxin, at concentrations which dramatically reduced the amplitude of whole-cell GABA currents, did not alter the spectral time constants or single-channel conductance estimated by analysis of GABA-activated current noise. This was observed at potentials both negative and positive to the GABA reversal potential (i.e. for both inward and outward GABA currents). In control conditions, the slow and fast time constants from GABA noise were 40 +/- 14 ms and 2 +/- 0.4 ms, while the estimated single-channel conductance was 14 +/- 2 pS. In the presence of picrotoxin, the time constants and estimated single-channel conductance were 41 +/- 5 ms, 2.7 +/- 0.6 ms and 15 +/- 2.3 pS. 3. Picrotoxin did not alter the shape of the whole-cell GABA current-voltage relationship, indicating that the steady-state block was not voltage dependent. The lack of effect of picrotoxin on the GABA noise spectra and the lack of outward rectification makes it unlikely that picrotoxin acts by a simple voltage-dependent (or voltage-independent) channel blocking mechanism. In the presence of picrotoxin the reversal potential for GABA remained at approximately 0 mV in symmetrical chloride. 4. Distributions of total burst durations, obtained from single-channel records with low concentrations of GABA, were fitted with three or four exponential components. Picrotoxin had no consistent effect on the time constants of the total burst length distributions. It also did not alter the amplitude of the main conductance state. However, picrotoxin did reduce the frequency of channel openings. 5. The application of brief ionophoretic pulses of GABA, to cells under whole-cell voltage clamp, revealed that the rate of onset of block by picrotoxin was accelerated in the presence of GABA. In the absence of agonist, picrotoxin produced a more slowly equilibrating block. 6. Our data are consistent with a mechanism whereby picrotoxin binds preferentially to an agonist bound form of the receptor and stabilizes an agonist-bound shut state. This could, for example, mean that picrotoxin enhances the occurrence of a desensitized state or an allosterically blocked state.

Full text

PDF
191

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adams P. R., Constanti A., Banks F. W. Opposing actions of convulsants and anticonvulsants on GABA responses of crayfish stretch receptors. Adv Biochem Psychopharmacol. 1981;29:369–378. [PubMed] [Google Scholar]
  2. Adams P. R. Drug blockade of open end-plate channels. J Physiol. 1976 Sep;260(3):531–552. doi: 10.1113/jphysiol.1976.sp011530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Akaike N., Hattori K., Oomura Y., Carpenter D. O. Bicuculline and picrotoxin block gamma-aminobutyric acid-gated Cl- conductance by different mechanisms. Experientia. 1985 Jan 15;41(1):70–71. doi: 10.1007/BF02005880. [DOI] [PubMed] [Google Scholar]
  4. Akaike N., Inoue M., Krishtal O. A. 'Concentration-clamp' study of gamma-aminobutyric-acid-induced chloride current kinetics in frog sensory neurones. J Physiol. 1986 Oct;379:171–185. doi: 10.1113/jphysiol.1986.sp016246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Barker J. L., McBurney R. N., Mathers D. A. Convulsant-induced depression of amino acid responses in cultured mouse spinal neurones studied under voltage clamp. Br J Pharmacol. 1983 Dec;80(4):619–629. doi: 10.1111/j.1476-5381.1983.tb10051.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bowery N. G., Brown D. A. Depolarizing actions of gamma-aminobutyric acid and related compounds on rat superior cervical ganglia in vitro. Br J Pharmacol. 1974 Feb;50(2):205–218. doi: 10.1111/j.1476-5381.1974.tb08563.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Colquhoun D., Hawkes A. G. On the stochastic properties of bursts of single ion channel openings and of clusters of bursts. Philos Trans R Soc Lond B Biol Sci. 1982 Dec 24;300(1098):1–59. doi: 10.1098/rstb.1982.0156. [DOI] [PubMed] [Google Scholar]
  8. Colquhoun D., Sakmann B. Fast events in single-channel currents activated by acetylcholine and its analogues at the frog muscle end-plate. J Physiol. 1985 Dec;369:501–557. doi: 10.1113/jphysiol.1985.sp015912. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Constanti A., Nistri A. A comparative study of the action of gamma-aminobutyric acid and piperazine on the lobster muscle fibre and the frog spinal cord. Br J Pharmacol. 1976 Jul;57(3):347–358. doi: 10.1111/j.1476-5381.1976.tb07673.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Constanti A. The "mixed" effect of picrotoxin on the GABA dose/conductance relation recorded from lobster muscle. Neuropharmacology. 1978 Mar;17(3):159–167. doi: 10.1016/0028-3908(78)90095-3. [DOI] [PubMed] [Google Scholar]
  11. Cull-Candy S. G., Mathie A. Ion channels activated by acetylcholine and gamma-aminobutyric acid in freshly dissociated sympathetic neurones of the rat. Neurosci Lett. 1986 May 23;66(3):275–280. doi: 10.1016/0304-3940(86)90031-5. [DOI] [PubMed] [Google Scholar]
  12. Cull-Candy S. G., Mathie A., Powis D. A. Acetylcholine receptor channels and their block by clonidine in cultured bovine chromaffin cells. J Physiol. 1988 Aug;402:255–278. doi: 10.1113/jphysiol.1988.sp017203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Cull-Candy S. G., Usowicz M. M. Whole-cell current noise produced by excitatory and inhibitory amino acids in large cerebellar neurones of the rat. J Physiol. 1989 Aug;415:533–553. doi: 10.1113/jphysiol.1989.sp017735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Enna S. J., Collins J. F., Snyder S. H. Stereospecificity and structure--activity requirements of GABA receptor binding in rat brain. Brain Res. 1977 Mar 18;124(1):185–190. doi: 10.1016/0006-8993(77)90878-2. [DOI] [PubMed] [Google Scholar]
  15. Fujimoto M., Okabayashi T. Effect of picrotoxin on benzodiazepine receptors and GABA receptors with reference to the effect of C1- ion. Life Sci. 1981 Feb 23;28(8):895–901. doi: 10.1016/0024-3205(81)90051-5. [DOI] [PubMed] [Google Scholar]
  16. Gallagher J. P., Higashi H., Nishi S. Characterization and ionic basis of GABA-induced depolarizations recorded in vitro from cat primary afferent neurones. J Physiol. 1978 Feb;275:263–282. doi: 10.1113/jphysiol.1978.sp012189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Greenlee D. V., Van Ness P. C., Olsen R. W. Gamma-aminobutyric acid binding in mammalian brain: receptor-like specificity of sodium-independent sites. J Neurochem. 1978 Oct;31(4):933–938. doi: 10.1111/j.1471-4159.1978.tb00130.x. [DOI] [PubMed] [Google Scholar]
  18. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  19. Howe J. R., Colquhoun D., Cull-Candy S. G. On the kinetics of large-conductance glutamate-receptor ion channels in rat cerebellar granule neurons. Proc R Soc Lond B Biol Sci. 1988 May 23;233(1273):407–422. doi: 10.1098/rspb.1988.0030. [DOI] [PubMed] [Google Scholar]
  20. Jackson M. B., Lecar H., Mathers D. A., Barker J. L. Single channel currents activated by gamma-aminobutyric acid, muscimol, and (-)-pentobarbital in cultured mouse spinal neurons. J Neurosci. 1982 Jul;2(7):889–894. doi: 10.1523/JNEUROSCI.02-07-00889.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Jarboe C. H., Poerter L. A., Buckler R. T. Structural aspects of picrotoxinin action. J Med Chem. 1968 Jul;11(4):729–731. doi: 10.1021/jm00310a020. [DOI] [PubMed] [Google Scholar]
  22. Kudo Y., Niwa H., Tanaka A., Yamada K. Actions of picrotoxinin and related compounds on the frog spinal cord: the role of a hydroxyl-group at the 6-position in antagonizing the actions of amino acids and presynaptic inhibition. Br J Pharmacol. 1984 Feb;81(2):373–380. doi: 10.1111/j.1476-5381.1984.tb10088.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Macdonald R. L., Rogers C. J., Twyman R. E. Kinetic properties of the GABAA receptor main conductance state of mouse spinal cord neurones in culture. J Physiol. 1989 Mar;410:479–499. doi: 10.1113/jphysiol.1989.sp017545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Maksay G., Ticku M. K. GABA, depressants and chloride ions affect the rate of dissociation of 35S-t-butylbicyclophosphorothionate binding. Life Sci. 1985 Dec 9;37(23):2173–2180. doi: 10.1016/0024-3205(85)90568-5. [DOI] [PubMed] [Google Scholar]
  25. Mathers D. A. Spontaneous and GABA-induced single channel currents in cultured murine spinal cord neurons. Can J Physiol Pharmacol. 1985 Oct;63(10):1228–1233. doi: 10.1139/y85-203. [DOI] [PubMed] [Google Scholar]
  26. Neher E., Steinbach J. H. Local anaesthetics transiently block currents through single acetylcholine-receptor channels. J Physiol. 1978 Apr;277:153–176. doi: 10.1113/jphysiol.1978.sp012267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Newland C. F., Colquhoun D., Cull-Candy S. G. Single channels activated by high concentrations of GABA in superior cervical ganglion neurones of the rat. J Physiol. 1991 Jan;432:203–233. doi: 10.1113/jphysiol.1991.sp018382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Ogden D. C., Colquhoun D. Ion channel block by acetylcholine, carbachol and suberyldicholine at the frog neuromuscular junction. Proc R Soc Lond B Biol Sci. 1985 Sep 23;225(1240):329–355. doi: 10.1098/rspb.1985.0065. [DOI] [PubMed] [Google Scholar]
  29. Porter L. A. Picrotoxinin and related substances. Chem Rev. 1967 Aug;67(4):441–464. doi: 10.1021/cr60248a004. [DOI] [PubMed] [Google Scholar]
  30. Quast U., Brenner O. Modulation of [3H]muscimol binding in rat cerebellar and cerebral cortical membranes by picrotoxin, pentobarbitone, and etomidate. J Neurochem. 1983 Aug;41(2):418–425. doi: 10.1111/j.1471-4159.1983.tb04758.x. [DOI] [PubMed] [Google Scholar]
  31. Sakmann B., Hamill O. P., Bormann J. Patch-clamp measurements of elementary chloride currents activated by the putative inhibitory transmitter GABA and glycine in mammalian spinal neurons. J Neural Transm Suppl. 1983;18:83–95. [PubMed] [Google Scholar]
  32. Segal M., Barker J. L. Rat hippocampal neurons in culture: voltage-clamp analysis of inhibitory synaptic connections. J Neurophysiol. 1984 Sep;52(3):469–487. doi: 10.1152/jn.1984.52.3.469. [DOI] [PubMed] [Google Scholar]
  33. Sigel E., Baur R. Allosteric modulation by benzodiazepine receptor ligands of the GABAA receptor channel expressed in Xenopus oocytes. J Neurosci. 1988 Jan;8(1):289–295. doi: 10.1523/JNEUROSCI.08-01-00289.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Simmonds M. A. Classification of some GABA antagonists with regard to site of action and potency in slices of rat cuneate nucleus. Eur J Pharmacol. 1982 Jun 4;80(4):347–358. doi: 10.1016/0014-2999(82)90080-2. [DOI] [PubMed] [Google Scholar]
  35. Squires R. F., Casida J. E., Richardson M., Saederup E. [35S]t-butylbicyclophosphorothionate binds with high affinity to brain-specific sites coupled to gamma-aminobutyric acid-A and ion recognition sites. Mol Pharmacol. 1983 Mar;23(2):326–336. [PubMed] [Google Scholar]
  36. Supavilai P., Mannonen A., Collins J. F., Karobath M. Anion-dependent modulation of [3H]muscimol binding and of GABA-stimulated [3H]flunitrazepam binding by picrotoxin and related CNS convulsants. Eur J Pharmacol. 1982 Jul 30;81(4):687–691. doi: 10.1016/0014-2999(82)90362-4. [DOI] [PubMed] [Google Scholar]
  37. Van Renterghem C., Bilbe G., Moss S., Smart T. G., Constanti A., Brown D. A., Barnard E. A. GABA receptors induced in Xenopus oocytes by chick brain mRNA: evaluation of TBPS as a use-dependent channel-blocker. Brain Res. 1987 Apr;388(1):21–31. doi: 10.1016/0169-328x(87)90017-9. [DOI] [PubMed] [Google Scholar]
  38. Weiss D. S., Magleby K. L. Gating scheme for single GABA-activated Cl- channels determined from stability plots, dwell-time distributions, and adjacent-interval durations. J Neurosci. 1989 Apr;9(4):1314–1324. doi: 10.1523/JNEUROSCI.09-04-01314.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Yakushiji T., Tokutomi N., Akaike N., Carpenter D. O. Antagonists of GABA responses, studied using internally perfused frog dorsal root ganglion neurons. Neuroscience. 1987 Sep;22(3):1123–1133. doi: 10.1016/0306-4522(87)92987-3. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES